Clausen T, Nielsen O B
Institute of Physiology, University of Aarhus, Denmark.
Acta Physiol Scand. 1994 Dec;152(4):365-73. doi: 10.1111/j.1748-1716.1994.tb09818.x.
In skeletal muscle, the excitation induced influx of Na+ and efflux of K+ may be sufficient to exceed the activity or even the capacity of the available Na+,K(+)-pumps. This leads to a rise in intracellular Na+ and extracellular K+. Both events interfere with excitability and may present important limitations for the continuation of contractile activity. Furthermore, inhibition of the Na+,K(+)-pump or reduction of the concentration of functional Na+,K(+)-pumps decrease excitability and the maintenance of force during continued stimulation. Conversely, in muscles where contractile force is inhibited by exposure to high extracellular K+, acute stimulation of the Na+,K(+)-pump with catecholamines, CGRP or insulin leads to a rapid recovery of force. The large passive fluxes of Na+ and K+ associated with excitation constitute the major drive on the activity of the Na+,K(+)-pump, giving rise to up to 20-fold stimulation of the transport rate. In keeping with this, training induces an upregulation of the total concentration of Na+,K(+)-pumps in skeletal muscle. The activity and the capacity of the Na+,K(+)-pump are important limiting factors determining the maintenance of excitability and contractile performance.
在骨骼肌中,兴奋诱导的Na⁺内流和K⁺外流可能足以超过可用Na⁺,K⁺-ATP酶的活性甚至能力。这会导致细胞内Na⁺浓度升高和细胞外K⁺浓度升高。这两个事件都会干扰兴奋性,并可能对收缩活动的持续进行构成重要限制。此外,抑制Na⁺,K⁺-ATP酶或降低功能性Na⁺,K⁺-ATP酶的浓度会降低兴奋性以及在持续刺激期间维持力量的能力。相反,在因暴露于高细胞外K⁺浓度而使收缩力受到抑制的肌肉中,用儿茶酚胺、降钙素基因相关肽(CGRP)或胰岛素急性刺激Na⁺,K⁺-ATP酶会导致力量迅速恢复。与兴奋相关的大量Na⁺和K⁺被动通量是驱动Na⁺,K⁺-ATP酶活性的主要因素,可使转运速率提高多达20倍。与此一致的是,训练会导致骨骼肌中Na⁺,K⁺-ATP酶总浓度上调。Na⁺,K⁺-ATP酶的活性和能力是决定兴奋性维持和收缩性能的重要限制因素。